Canonical Allele Identifier: CA2271191740
Gene: APOH HGNC NCBI

Linked Data

dbSNP Id: rs1324039036

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66227933A>G , CM000679.2:g.66227933A>G GRCh38
NC_000017.10:g.64224051A>G , CM000679.1:g.64224051A>G GRCh37
NC_000017.9:g.61654513A>G NCBI36
NG_012045.1:g.6506T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000205948.11:c.241+87T>C MANE Select ENSP00000205948.6:n.241+87T>C
ENST00000205948.10:c.241+87T>C ENSP00000205948.6:n.241+87T>C
ENST00000577982.1:c.241+87T>C ENSP00000464301.1:n.241+87T>C
ENST00000581797.5:c.61+87T>C ENSP00000463553.1:n.61+87T>C
NM_000042.2:c.241+87T>C NP_000033.2:n.241+87T>C
NM_000042.3:c.241+87T>C MANE Select NP_000033.2:n.241+87T>C